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Merck
CN

74989

Octylamine

analytical standard

Synonym(s):

1-Aminooctane, n-Octylamine, Caprylamine

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About This Item

Linear Formula:
CH3(CH2)7NH2
CAS Number:
111-86-4
Molecular Weight:
129.24
EC Number:
203-916-0
UNSPSC Code:
41116107
PubChem Substance ID:
329766025
Beilstein/REAXYS Number:
1679227
MDL number:
MFCD00008247

Key Documents

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InChI key

IOQPZZOEVPZRBK-UHFFFAOYSA-N

InChI

1S/C8H19N/c1-2-3-4-5-6-7-8-9/h2-9H2,1H3

SMILES string

CCCCCCCCN

grade

analytical standard

vapor pressure

1 mmHg ( 20 °C)

assay

≥99.5% (GC)

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

impurities

≤0.2% water

Quality Level

100

bp

175-177 °C (lit.)

mp

−5-−1 °C (lit.)

density

0.782 g/mL at 25 °C (lit.)

application(s)

environmental

format

neat

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Application

Octylamine may be used as an ion pairing reagent for the separation and determination of biogenic amines and precursor aminoacids in various food samples using ion-pair high-performance liquid chromatography technique.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Acute Tox. 4 Inhalation - Aquatic Acute 1 - Aquatic Chronic 2 - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1A - STOT SE 3

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

140.0 °F - closed cup

flash_point_c

60 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

Regulatory Information

危险化学品
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Certificates of Analysis (COA)

Lot/Batch Number
0000092854
0000070333
0000021703
0000066450
0000055384

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Ion-pair HPLC determination of biogenic amines and precursor aminoacids. Application of a method based on simultaneous use of heptanesulphonate and octylamine to some foods
Arlorio.M, et al.
Chromatographia, 48(11-12), 763-769 (1998)
Jin-Young Lee et al.
Journal of hazardous materials, 168(1), 424-429 (2009-03-17)
Liquid-liquid extraction/separation of platinum(IV) and rhodium(III) from acidic chloride solutions was carried out using tri-iso-octylamine (Alamine 308) as an extractant diluted in kerosene. The percentage extraction of platinum(IV) and rhodium(III) increased with increase in acid concentration up to 8 mol
Erin Harleton et al.
The Journal of pharmacology and experimental therapeutics, 310(3), 1011-1019 (2004-05-04)
The anticancer drug N,N,"N"-triethylenethiophosphoramide (tTEPA) inactivated CYP2B6 and CYP2B1 in the reconstituted system in a time-, concentration-, and NADPH-dependent manner indicative of mechanism-based inactivation. The KI value for the inactivation of CYP2B1 was 38 microM, the kinact was 0.3 min(-1)
Kristine Spildo et al.
Journal of colloid and interface science, 252(2), 470-472 (2005-11-18)
The adsorption of octanoic acid (Octac) and octylamine (Octam) onto silica from isooctane solutions has been studied, both from individual solutions of Octac and Octam and from mixtures of the two in isooctane. The results show that Octam has a
Monica Moreno et al.
Journal of the American Chemical Society, 133(12), 4389-4397 (2011-03-03)
Palladium monolayer-protected clusters (MPCs) coated with octylamines (C8NH(2)), hexanethiolates (C6S), and mixed monolayers of C8NH(2) and C6S exhibit significantly different reactivities with hydrogen gas, depending on the relative amounts of the two ligands coating the Pd nanoparticle surface, as determined
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